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Details
Link-It Detail - Human Phenotype - Abnormality of adrenal morphology
Debug Stats
  • ### Total Build Time: 35 ms 25.438 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 454 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.666 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.169 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 19.784 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of adrenal morphology HP:0011732
Parents (1)
img Abnormality of the adrenal glands HP:0000834
Children (8)
img Adrenocortical abnormality HP:0000849
img Adrenocortical cytomegaly HP:0008186
img Adrenal calcification HP:0010512
img Neoplasm of the adrenal gland HP:0100631
img Adrenal hypoplasia HP:0000835
img Adrenal hyperplasia HP:0008221
img Adrenal gland dysgenesis HP:0008216
img Ectopic adrenal gland HP:0011742
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the adrenal glands HP:0000834
Genes (81)

Species:
human : 81
Page Size
Current 25
  Page 1 of 4
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanHYLS1219844hydrolethalus syndrome 1
img HP RolledUp, OMIM ID: 236680
HumanHPE6117190holoprosencephaly 6
img HP RolledUp, OMIM ID: 236100
HumanLHX489884LIM homeobox 4
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 130650
HumanPEX2655670peroxisomal biogenesis factor 26
img HP RolledUp, OMIM ID: 214100
HumanMKS154903Meckel syndrome, type 1
img HP RolledUp, OMIM ID: 249000
HumanWNT454361wingless-type MMTV integration site family, member 4
img HP RolledUp, OMIM ID: 611812
HumanPDE11A50940phosphodiesterase 11A
HumanNSDHL50814NAD(P) dependent steroid dehydrogenase-like
img HP RolledUp, OMIM ID: 308050
HumanICK22858intestinal cell (MAK-like) kinase
img HP RolledUp, OMIM ID: 612651
HumanKCNQ1OT110984KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanZMPSTE2410269zinc metallopeptidase STE24
img HP RolledUp, OMIM ID: 275210
HumanTBX199095T-box 19
img HP RolledUp, OMIM ID: 201400
HumanAIP9049aryl hydrocarbon receptor interacting protein
img HP RolledUp, OMIM ID: 219090
HumanPDE8B8622phosphodiesterase 8B
img HP RolledUp, OMIM ID: 614190
HumanPEX38504peroxisomal biogenesis factor 3
img HP RolledUp, OMIM ID: 214100
HumanAAAS8086achalasia, adrenocortical insufficiency, alacrimia
HumanLHX38022LIM homeobox 3
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
HumanWT27491Wilms tumor 2
HumanWNT37473wingless-type MMTV integration site family, member 3
img HP RolledUp, OMIM ID: 273395
HumanTP537157tumor protein p53
HumanTNXB7148tenascin XB
img HP RolledUp, OMIM ID: 606408
HumanTHM7063thymoma
img HP RolledUp, OMIM ID: 274230
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011732Abnormality of adrenal morphology0self